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FDA product code LQJ · Class 2 · Ophthalmic

5
Registered devices
11
Adverse events
1
Recalls
13
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2005-09-02Alcon Research, LtdUnknown residue noted on suface of flap irrigators incorporated into cusom paks.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.